首页|秀珍菇3-羟基-3-甲基戊二酰辅酶A还原酶基因的克隆及表达分析

秀珍菇3-羟基-3-甲基戊二酰辅酶A还原酶基因的克隆及表达分析

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为获得秀珍菇3-羟基-3-甲基戊二酰辅酶A还原酶(HMGR)全长基因,并分析该基因在秀珍菇正常状态及热胁迫处理下的表达差异,对秀珍菇进行RNA测序(RNA-seq),经生物信息学分析筛选获得HMGR全长基因(命名为Pphg1),并利用荧光定量PCR(qRT-PCR)的方法,分析该基因在秀珍菇不同温度处理下的表达情况.结果表明,获得的Pphg1 全长由 4 059个核苷酸组成,编码 1 352个氨基酸,其蛋白分子质量约 144.04 kDa.经qRT-PCR检测,该基因在秀珍菇受热胁迫后表达量升高.本研究中首次克隆并获得秀珍菇HMGR基因全长cDNA,推测其与秀珍菇热胁迫应答相关,为阐明秀珍菇体内次生代谢产物合成的分子机制及其分子育种提供科学依据.
Cloning and Expression Analysis of 3-hydroxy-3-methylglutaryl-CoA Reductase(HMGR)Gene of Pleurotus pulmonarius
In order to obtain the full-length 3-hydroxy-3-methylglutaryl-CoA reductase(HMGR)gene and analyze the gene expression differences Pleurotus pulmonarius in normal temperature and heat stress condition,the full-length HMGR gene(named Pphg1)was isolated through RNA sequencing,and qRT-PCR was used to detect the gene expression levels in different temperature treatment of P.pulmonarius.The full-length of Pphg1 has an open reading frame of 4 059 bp.The deduced amino acid sequence of Pphg1 has 1 352 amino acid residues which form a 144.04 kDa polypeptide.qRT-PCR indicated that Pphg1 was expressed at a high level in high temperature treatment.The cDNA encoding HMGR gene from P.pulmonarius is cloned and reported for the first time.Pphg1 is supposed to be the crucial enzyme in responding to heat stress.This study provides a scientific basis for exploring the development mechanism and its molecular breeding of P.pulmonarius.

Pleurotus pulmonariuscloneqRT-PCR3-hydroxy-3-methylglutaryl-coa reductase gene

周小华、林佳瑶、陆娜

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桐庐县农业技术推广中心,浙江 杭州 311500

杭州市农业科学研究院,浙江 杭州 311024

秀珍菇 克隆 RT-PCR 3-羟基-3-甲基戊二酰辅酶A还原酶基因

杭州市农技(食用菌)专家首席工作室项目(2022)

2024

中国食用菌
中国食用菌协会 中华全国供销合作总社昆明食用菌研究所 全国食用菌科技情报中心站

中国食用菌

影响因子:0.574
ISSN:1003-8310
年,卷(期):2024.43(1)
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